(E)-3-Hexadecen-1-ol | 128999-42-8

• 分子结构分类: 有机化合物 - 脂质和类脂质分子 - 脂肪酰基
• 英文名称: (E)-3-Hexadecen-1-ol
• 英文别名: (E)-hexadec-3-en-1-ol；2-(Benzylsulfonyl)-4-methoxybenzamide
• CAS: 128999-42-8
• 化学式: C₁₆H₃₂O
• 分子量: 240.429
• InChiKey: OKOGACXRQKCGEH-BUHFOSPRSA-N

物化性质

• 沸点：
  336.6±11.0 °C(Predicted)
• 密度：
  0.847±0.06 g/cm3(Predicted)
• 保留指数：
  1865

计算性质

• 辛醇/水分配系数(LogP)：
  6.7
• 重原子数：
  17
• 可旋转键数：
  13
• 环数：
  0.0
• sp3杂化的碳原子比例：
  0.88
• 拓扑面积：
  20.2
• 氢给体数：
  1
• 氢受体数：
  1

反应信息

• 作为反应物：
  描述：

  (E)-3-Hexadecen-1-ol 在 甲基磺酰胺 、 camphor-10-sulfonic acid 、 sodium hydride 、 二甲基亚砜 、 氢化奎尼定 1,4-(2,3-二氮杂萘)二醚 作用下， 以 二氯甲烷 、 水 、 N,N-二甲基甲酰胺 、 叔丁醇 为溶剂， 反应 44.83h， 生成 (3R,4R)-1-O-benzyl-3,4-O-isopropylidenehexadecane-1,3,4-triol
  参考文献：
  名称：

  Synthesis of (4R,12S,15S,16S,19R,20R,34S)-Muricatetrocin and (4R,12R,15S,16S,19R,20R,34S)-Muricatetrocin, Two Potent Inhibitors of Mitochondrial Complex I

  摘要：

  DOI：

  10.1002/1099-0690(200006)2000:12<2207::aid-ejoc2207>3.0.co;2-c
• 作为产物：
  描述：

  n-3-hexadecyn-1-ol 在 lithium aluminium tetrahydride 作用下， 以 二乙二醇二甲醚 为溶剂， 反应 8.0h， 以84%的产率得到(E)-3-Hexadecen-1-ol
  参考文献：
  名称：

  Metal/ammonia reduction of ethers of 3-decyn-1-ol: effects of structure and conditions on cleavage and rearrangement

  摘要：

  Reduction of the THP, ethyl, tert-butyl and tert-butyldimethylsilyl (TBDMS) ethers of 3-decyn-1-ol with sodium in ammonia/THF results in extensive hydrogenolysis of the carbon-oxygen bond and concomitant bond migration, producing a mixture of 2- and 3-decenes and a very low yield of the desired (E)-homoallylic ether. Reduction in the presence of 2-methyl-2-propanol led to excellent yields of the desired (E)-3-decenol ethers. The 4- and 5-decyn-1-ol ethers were reduced normally to the (E)-decen-1-ol ethers except in the case of the TBDMS ethers which were cleaved to the (E)-alcohols under some of the reaction conditions.

  DOI：

  10.1021/jo00071a014

文献信息

• Metal/ammonia reduction of ethers of 3-decyn-1-ol: effects of structure and conditions on cleavage and rearrangement
  作者：Robert E. Doolittle、Delrea G. Patrick、Robert H. Heath

  DOI：10.1021/jo00071a014

  日期：1993.9

  Reduction of the THP, ethyl, tert-butyl and tert-butyldimethylsilyl (TBDMS) ethers of 3-decyn-1-ol with sodium in ammonia/THF results in extensive hydrogenolysis of the carbon-oxygen bond and concomitant bond migration, producing a mixture of 2- and 3-decenes and a very low yield of the desired (E)-homoallylic ether. Reduction in the presence of 2-methyl-2-propanol led to excellent yields of the desired (E)-3-decenol ethers. The 4- and 5-decyn-1-ol ethers were reduced normally to the (E)-decen-1-ol ethers except in the case of the TBDMS ethers which were cleaved to the (E)-alcohols under some of the reaction conditions.
• Synthesis of (4R,12S,15S,16S,19R,20R,34S)-Muricatetrocin and (4R,12R,15S,16S,19R,20R,34S)-Muricatetrocin, Two Potent Inhibitors of Mitochondrial Complex I
  作者：Stefan Bäurle、Ulf Peters、Thorsten Friedrich、Ulrich Koert

  DOI：10.1002/1099-0690(200006)2000:12<2207::aid-ejoc2207>3.0.co;2-c

  日期：2000.6